US2026048057A1PendingUtilityA1
Anti-ischemic compositions
Est. expiryAug 5, 2039(~13 yrs left)· nominal 20-yr term from priority
A61K 38/012A61K 9/16A01N 1/126A61P 7/08A61K 31/519A61K 35/62A61K 38/42A61K 38/05A61P 9/10
60
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Claims
Abstract
Described herein are compositions for use in medicine as anti-ischemic organ storage and perfusion solutions.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of preparing a composition, comprising:
combining a purified erythrocruorin with 5-methyltetrahydrofolate, 5-formyltetrahydrofolate, or 5-methyltetrahydrofolate and 5-formyltetrahydrofolate, and optionally 5,6,7,8-tetrahydrobiopterin.
2 . The method of claim 1 , wherein the composition is stored as a liquid.
3 . The method of claim 1 , wherein the composition is reduced to a paste.
4 . The method of claim 1 , wherein the composition is lyophilized to a powder.
5 . The method of claim 1 , wherein the purified erythrocruorin is combined with 0.001 to 500 μmol/L 5-methyltetrahydrofolate and 0.001 to 500 μmol/L 5,6,7,8-tetrahydrobiopterin.
6 . The method of claim 5 , wherein the composition is stored as a liquid.
7 . The method of claim 5 , wherein the composition is reduced to a paste.
8 . The method of claim 5 , wherein the composition is lyophilized to a powder.
9 . The method of claim 1 , wherein the purified erythrocruorin is combined with 0.001 to 500 μmol/L 5-formyltetrahydrofolate and 0.001 to 500 μmol/L 5,6,7,8-tetrahydrobiopterin.
10 . The method of claim 9 , wherein the composition is stored as a liquid.
11 . The method of claim 9 , wherein the composition is reduced to a paste.
12 . The method of claim 9 , wherein the composition is lyophilized to a powder.
13 . The method of claim 1 , wherein the purified erythrocruorin is combined with 0.001 to 500 μmol/L 5-methyltetrahydrofolate, 0.001 to 500μmol/L 5-formyltetrahydrofolate and 0.001 to 500 μmol/L 5,6,7,8-tetrahydrobiopterin.
14 . The method of claim 13 , wherein the composition is stored as a liquid.
15 . The method of claim 13 , wherein the composition is reduced to a paste.
16 . The method of claim 13 , wherein the composition is lyophilized to a powder.
17 . The method of claim 1 , wherein the purified erythrocruorin is a purified annelid erythrocruorin.
18 . The method of claim 1 , wherein the purified erythrocruorin is a purified arthropod erythrocruorin.
19 . The method of claim 1 , wherein the purified erythrocruorin is a purified insect erythrocruorin.
20 . The method of claim 1 , wherein the purified erythrocruorin is a purified Lumbricus terrestris erythrocruorin.Join the waitlist — get patent alerts
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